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62 Astrix Product Manufacturing Jobs Hiring Near You

Astrix Inc

QA Associate - cGMP

Wilmington, OH · On-site

$24 - $26/hr

Experience with quality systems administration in drug product manufacturing and quality control environments. * Strong written, verbal communication, and computer skills. * Physical & On-Site ...

Astrix Inc

Manufacturing Associate

Cary, NC · On-site

We are seeking a motivated Manufacturing Associate with 2+ years of experience in cell and gene therapy production or similar biomanufacturing space. The ideal candidate holds a BS degree and has ...

Astrix Inc

Manufacturing Engineer I

Duluth, GA · On-site

$67K - $86K/yr

Analyze workflows, layouts, production data, and process performance * Support process quality, testing, and continuous improvement * Prepare technical reports and analyze manufacturing trends * Work ...

Astrix Inc

Manufacturing Visual Inspection

Fremont, CA · On-site

Inspecting drug products for quality defects, completing batch documentation, operating manufacturing and MES systems, maintaining equipment logs, supporting packaging and filling operations, and ...

Astrix Inc

Process Engineer (Manufacturing)

Atlanta, GA · On-site

$115K - $135K/yr

Process Engineer (Manufacturing) Salary: $115,000 - $135,000 (DOE) Job type: Full- time Location ... Analyze operational and production data to identify inefficiencies and determine root causes

Astrix Inc.

Cosmetic Manufacturing Buyer

Livermore, CA · On-site

$55 - $69/hr

... manufacturing organization. The Buyerwill work with a wide range of vendors and suppliers, from ... This person works with suppliers to determine which products will be used in production and how ...

Astrix Inc

Chemist I

Cincinnati, OH · On-site

$25/hr

Review batch and production documentation for accuracy and GMP compliance. * Support manufacturing and quality improvement initiatives through laboratory testing. * Maintain laboratory ...

Astrix Inc

QA Inspector

Chino, CA · On-site

Pay Rate Low: 21 | Pay Rate High: 25 Position Overview We are partnering with an established consumer products manufacturer to place a detail-oriented Quality Control Inspector on their production ...

Astrix Inc

Chemist I

Cincinnati, OH · On-site

$25/hr

Review batch and production documentation for accuracy and GMP compliance. * Support manufacturing and quality improvement initiatives through laboratory testing. * Maintain laboratory ...

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What makes Astrix an attractive place to work?

Astrix is a well-established company in the industry, known for its commitment to delivering innovative solutions and exceptional customer experiences. The company's workplace is characterized by a collaborative environment that fosters creativity, open communication, and a culture of continuous learning, with opportunities for professional growth and development. Joining Astrix offers the chance to be part of a dynamic team that values innovation, teamwork, and excellence, with opportunities to make a meaningful impact and contribute to the company's continued success.

What are the most popular job types at Astrix?

    What are the most popular jobs at Astrix?

    What are the most popular categories at Astrix?

    Infographic showing various Product Manufacturing job openings at Astrix in the United States as of August 2026, with employment types broken down into 58% Full Time, 1% Part Time, 32% Contract, and 9% Nights. Highlights an 96% Physical, and 4% Remote job distribution.

    QA Associate - cGMP

    Astrix Inc

    Wilmington, OH • On-site

    $24 - $26/hr

    Contractor

    Re-posted 29 days ago

    Job description

    Pay Rate Low: 24 | Pay Rate High: 26
    Our client focuses on therapies for widespread, chronic diseases, such as central nervous system disorders, addiction, diabetes and autoimmune disorders, where we feel we can make the greatest impact.
    Position: Quality Assurance Associate
    Pay Rate: $24 - $26/ hour
    Location: Wilmington, OH 45177
    Schedule: Monday-Friday 1 st shift
    Type: Contract to hire
    Position Summary
    The position will perform general QA activities using their ability as a skilled contributor in completing tasks where judgement is required in resolving problems and making recommendations. Works on problems of a diverse scope where problem solving is required. Receives general oversight and guidance on approaches to complete project related tasks. The ideal candidate will apply skilled problem-solving abilities under general supervision to ensure continuous adherence to current Good Manufacturing Practices (cGMP).
    Key Responsibilities
    • Manufacturing & Shop-Floor Support: Conduct on-the-floor batch record reviews, visual equipment inspections, equipment releases, status tagging, work order reviews, and room/utility checklist verifications.
    • Compliance & Monitoring: Monitor cGMP compliance throughout the facility and product lifecycle; partner with plant personnel to enforce compliance standards.
    • Investigation & Corrective Actions: Follow up on preventive and corrective actions (CAPA) related to deviations, laboratory investigations, and environmental excursions.
    • Documentation: Review logbooks, facility records, and production documents for accuracy and completeness.
    • Operational Flexibility: Provide backup coverage for other Quality Assurance roles as needed.

    Qualifications & Requirements
    • Education & Experience:
      • Bachelor's degree in a scientific discipline (or equivalent experience). Relevant pharmaceutical industry experience may be substituted for a degree.
      • Minimum of 1 year of Quality Assurance experience in the pharmaceutical industry preferred.
    • Technical Skills & Knowledge:
      • Working knowledge of US Drug Product cGMP regulations and industry guidelines.
      • Experience with quality systems administration in drug product manufacturing and quality control environments.
      • Strong written, verbal communication, and computer skills.
    • Physical & On-Site Requirements:
      • Ability to wear aseptic gowning and Powered Air-Purifying Respirator (PAPR) equipment for up to 4 consecutive hours.
      • Must successfully pass required health assessments prior to the start date.
      • Must pass all post-training assessments and certifications.
    Key Competencies
    • High attention to detail, organization, and problem-solving initiative.
    • Ability to prioritize and manage multiple open issues simultaneously in a fast-paced environment.
    • Strong work ethic, dependability, and a collaborative, team-oriented mindset.

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